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GRCh37/hg19 13q31.3(chr13:92719735-92817257)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000447240

Variant: GRCh37/hg19 13q31.3(chr13:92719735-92817257)x1

Type: Variant
Allele: GRCh37/hg19 13q31.3(chr13:92719735-92817257)x1 383795
Gene:
Type: copy number loss
Location: Chr13: 92719735 - 92817257 - assembly GRCh37
References: dbVar: nsv2775680
dbVar: nssv13650973

Condition

PhenotypeInstruction: See cases